{"title":"Development of cardiovascular and all-cause mortality risk prediction models for maintenance hemodialysis patients based on metabolomics.","authors":"Lian-Lian You, Cui Dong, Zhi-Hong Wang, Shuang Zhang, Yu Zhang, Ting-Ting Kuai, Jia Xiao, Shu-Xin Liu, Qing-Cheng Zeng","doi":"10.1186/s12882-025-04291-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The outcome of maintenance hemodialysis (MHD) remains poor, with cardiovascular death accounting for more than half of all-cause death cases. In this study, cardiovascular mortality and all-cause mortality prediction models were developed to investigate the predictive role of metabolites in MHD patients.</p><p><strong>Methods: </strong>Clinical and metabolomics data of 135 hemodialysis patients from a single center were collected with a 6-year follow-up. Univariate Cox regression and random forest were respectively applied to preliminarily screen clinical and metabolomics characteristics, followed by multivariate Cox regression for identifying features predicting cardiovascular or all-cause mortality. Multivariate Cox proportional regression risk models were constructed using clinical, metabolomics, and combined features. Subgroup survival differences were compared via risk score stratification.</p><p><strong>Results: </strong>The combined model showed significant superiority in predicting cardiovascular mortality (3-year AUC = 0.901, 5-year AUC = 0.876), surpassing the clinical-only model (0.868/0.826) and metabolomics-only model (0.659/0.641). For all-cause mortality, the combined model demonstrated modest improvement (0.859/0.834) but still outperformed the metabolomics model (0.534/0.653). Thirty 5-fold cross-validations confirmed stable performance. High-risk groups had significantly higher cumulative mortality than low-risk groups (p < 0.0001).</p><p><strong>Conclusion: </strong>The metabolomics-alone model showed limited predictive performance, but its synergistic integration with clinical indicators further improved the predictive performance of mortality risk models, particularly for cardiovascular mortality.</p>","PeriodicalId":9089,"journal":{"name":"BMC Nephrology","volume":"26 1","pages":"372"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Nephrology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12882-025-04291-0","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: The outcome of maintenance hemodialysis (MHD) remains poor, with cardiovascular death accounting for more than half of all-cause death cases. In this study, cardiovascular mortality and all-cause mortality prediction models were developed to investigate the predictive role of metabolites in MHD patients.
Methods: Clinical and metabolomics data of 135 hemodialysis patients from a single center were collected with a 6-year follow-up. Univariate Cox regression and random forest were respectively applied to preliminarily screen clinical and metabolomics characteristics, followed by multivariate Cox regression for identifying features predicting cardiovascular or all-cause mortality. Multivariate Cox proportional regression risk models were constructed using clinical, metabolomics, and combined features. Subgroup survival differences were compared via risk score stratification.
Results: The combined model showed significant superiority in predicting cardiovascular mortality (3-year AUC = 0.901, 5-year AUC = 0.876), surpassing the clinical-only model (0.868/0.826) and metabolomics-only model (0.659/0.641). For all-cause mortality, the combined model demonstrated modest improvement (0.859/0.834) but still outperformed the metabolomics model (0.534/0.653). Thirty 5-fold cross-validations confirmed stable performance. High-risk groups had significantly higher cumulative mortality than low-risk groups (p < 0.0001).
Conclusion: The metabolomics-alone model showed limited predictive performance, but its synergistic integration with clinical indicators further improved the predictive performance of mortality risk models, particularly for cardiovascular mortality.
期刊介绍:
BMC Nephrology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of kidney and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.